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Baseline Cerebrospinal Fluid α-Synuclein in Parkinson’s Disease Is Associated with Disease Progression and Cognitive Decline

Biomarkers are increasingly recognized as tools in the diagnosis and prognosis of neurodegenerative diseases. No fluid biomarker for Parkinson’s disease (PD) has been established to date, but α-synuclein, a major component of Lewy bodies in PD and dementia with Lewy bodies (DLB), has become a promis...

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Autores principales: Emdina, Anna, Hermann, Peter, Varges, Daniela, Nuhn, Sabine, Goebel, Stefan, Bunck, Timothy, Maass, Fabian, Schmitz, Matthias, Llorens, Franc, Kruse, Niels, Lingor, Paul, Mollenhauer, Brit, Zerr, Inga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140902/
https://www.ncbi.nlm.nih.gov/pubmed/35626415
http://dx.doi.org/10.3390/diagnostics12051259
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author Emdina, Anna
Hermann, Peter
Varges, Daniela
Nuhn, Sabine
Goebel, Stefan
Bunck, Timothy
Maass, Fabian
Schmitz, Matthias
Llorens, Franc
Kruse, Niels
Lingor, Paul
Mollenhauer, Brit
Zerr, Inga
author_facet Emdina, Anna
Hermann, Peter
Varges, Daniela
Nuhn, Sabine
Goebel, Stefan
Bunck, Timothy
Maass, Fabian
Schmitz, Matthias
Llorens, Franc
Kruse, Niels
Lingor, Paul
Mollenhauer, Brit
Zerr, Inga
author_sort Emdina, Anna
collection PubMed
description Biomarkers are increasingly recognized as tools in the diagnosis and prognosis of neurodegenerative diseases. No fluid biomarker for Parkinson’s disease (PD) has been established to date, but α-synuclein, a major component of Lewy bodies in PD and dementia with Lewy bodies (DLB), has become a promising candidate. Here, we investigated CSF α-synuclein in patients with PD (n = 28), PDD (n = 8), and DLB (n = 5), applying an electrochemiluminescence immunoassay. Median values were non-significantly (p = 0.430) higher in patients with PDD and DLB (287 pg/mL) than in PD (236 pg/mL). A group of n = 36 primarily non-demented patients with PD and PDD was clinically followed for up to two years. A higher baseline α-synuclein was associated with increases in Hoehn and Yahr classifications (p = 0.019) and Beck Depression Inventory scores (p < 0.001) as well as worse performance in Trail Making Test A (p = 0.017), Trail Making Test B (p = 0.043), and the Boston Naming Test (p = 0.002) at follow-up. Surprisingly, higher levels were associated with a better performance in semantic verbal fluency tests (p = 0.046). In summary, CSF α-synuclein may be a potential prognostic marker for disease progression, affective symptoms, and executive cognitive function in PD. Larger-scaled studies have to validate these findings and the discordant results for single cognitive tests in this exploratory investigation.
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spelling pubmed-91409022022-05-28 Baseline Cerebrospinal Fluid α-Synuclein in Parkinson’s Disease Is Associated with Disease Progression and Cognitive Decline Emdina, Anna Hermann, Peter Varges, Daniela Nuhn, Sabine Goebel, Stefan Bunck, Timothy Maass, Fabian Schmitz, Matthias Llorens, Franc Kruse, Niels Lingor, Paul Mollenhauer, Brit Zerr, Inga Diagnostics (Basel) Article Biomarkers are increasingly recognized as tools in the diagnosis and prognosis of neurodegenerative diseases. No fluid biomarker for Parkinson’s disease (PD) has been established to date, but α-synuclein, a major component of Lewy bodies in PD and dementia with Lewy bodies (DLB), has become a promising candidate. Here, we investigated CSF α-synuclein in patients with PD (n = 28), PDD (n = 8), and DLB (n = 5), applying an electrochemiluminescence immunoassay. Median values were non-significantly (p = 0.430) higher in patients with PDD and DLB (287 pg/mL) than in PD (236 pg/mL). A group of n = 36 primarily non-demented patients with PD and PDD was clinically followed for up to two years. A higher baseline α-synuclein was associated with increases in Hoehn and Yahr classifications (p = 0.019) and Beck Depression Inventory scores (p < 0.001) as well as worse performance in Trail Making Test A (p = 0.017), Trail Making Test B (p = 0.043), and the Boston Naming Test (p = 0.002) at follow-up. Surprisingly, higher levels were associated with a better performance in semantic verbal fluency tests (p = 0.046). In summary, CSF α-synuclein may be a potential prognostic marker for disease progression, affective symptoms, and executive cognitive function in PD. Larger-scaled studies have to validate these findings and the discordant results for single cognitive tests in this exploratory investigation. MDPI 2022-05-18 /pmc/articles/PMC9140902/ /pubmed/35626415 http://dx.doi.org/10.3390/diagnostics12051259 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Emdina, Anna
Hermann, Peter
Varges, Daniela
Nuhn, Sabine
Goebel, Stefan
Bunck, Timothy
Maass, Fabian
Schmitz, Matthias
Llorens, Franc
Kruse, Niels
Lingor, Paul
Mollenhauer, Brit
Zerr, Inga
Baseline Cerebrospinal Fluid α-Synuclein in Parkinson’s Disease Is Associated with Disease Progression and Cognitive Decline
title Baseline Cerebrospinal Fluid α-Synuclein in Parkinson’s Disease Is Associated with Disease Progression and Cognitive Decline
title_full Baseline Cerebrospinal Fluid α-Synuclein in Parkinson’s Disease Is Associated with Disease Progression and Cognitive Decline
title_fullStr Baseline Cerebrospinal Fluid α-Synuclein in Parkinson’s Disease Is Associated with Disease Progression and Cognitive Decline
title_full_unstemmed Baseline Cerebrospinal Fluid α-Synuclein in Parkinson’s Disease Is Associated with Disease Progression and Cognitive Decline
title_short Baseline Cerebrospinal Fluid α-Synuclein in Parkinson’s Disease Is Associated with Disease Progression and Cognitive Decline
title_sort baseline cerebrospinal fluid α-synuclein in parkinson’s disease is associated with disease progression and cognitive decline
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140902/
https://www.ncbi.nlm.nih.gov/pubmed/35626415
http://dx.doi.org/10.3390/diagnostics12051259
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